|Official Full Name||DnaJ (Hsp40) homolog, subfamily C, member 30|
|Background||This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.|
|Synonyms||DNAJC30; DnaJ (Hsp40) homolog, subfamily C, member 30; WBSCR18, Williams Beuren syndrome chromosome region 18; dnaJ homolog subfamily C member 30; DNAJC 30; WBSCR18; DnaJ (Hsp40) homolog subfamily C member 30; MGC12943; WBSCR 18; Williams Beuren syndrome chromosomal region 18 protein; Williams Beuren syndrome chromosome region 18; williams-Beuren syndrome chromosomal region 18 protein|
|Species||Cat.#||Product name||Source (Host)||Tag||Protein Length||Price|
dnajc30 involved in several pathways and played different roles in them. We selected most pathways dnajc30 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with dnajc30 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
|Pathway Name||Pathway Related Protein|
dnajc30 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by dnajc30 itself. We selected most functions dnajc30 had, and list some proteins which have the same functions with dnajc30. You can find most of the proteins on our site.
dnajc30 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with dnajc30 here. Most of them are supplied by our site. Hope this information will be useful for your research of dnajc30.